AVS Aria Cage — Class II medical device recall Z-0092-2019
Terminated recall by Stryker Spine, reported 2018-10-17, distributed nationwide. The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage.
| Recall number | Z-0092-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Spine, Allendale, NJ, United States |
| Recall initiated | 2018-08-13 |
| Classified | 2018-10-09 |
| Reported by FDA | 2018-10-17 |
| Terminated | 2019-05-23 |
| Distributed | Nationwide (US) |
| Quantity | 5 |
| Lot numbers | 7HX |
| Model numbers | 48753212 |
Product
AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral body fusion devices indicated for use with autogenous bone graft in patients with degenerative disc disease (DDD) at one level or two contiguous levels from L2 to S1 . The AVS¿ ARIA TM PEEK Spacers are intended to be used with supplemental fixation systems that have been cleared for use in the lumbosacral spine.
Reason for recall
The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0092-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.